Classifications

• • C—CHEMISTRY; METALLURGY
  • C13—SUGAR INDUSTRY
  • C13K—SACCHARIDES OBTAINED FROM NATURAL SOURCES OR BY HYDROLYSIS OF NATURALLY OCCURRING DISACCHARIDES, OLIGOSACCHARIDES OR POLYSACCHARIDES
  • C13K1/00—Glucose; Glucose-containing syrups
  • C13K1/10—Crystallisation
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
  • C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
  • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
  • A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
  • A01N43/16—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/16—Organic compounds
  • C11D3/20—Organic compounds containing oxygen
  • C11D3/22—Carbohydrates or derivatives thereof
  • C11D3/221—Mono, di- or trisaccharides or derivatives thereof
• • C—CHEMISTRY; METALLURGY
  • C13—SUGAR INDUSTRY
  • C13K—SACCHARIDES OBTAINED FROM NATURAL SOURCES OR BY HYDROLYSIS OF NATURALLY OCCURRING DISACCHARIDES, OLIGOSACCHARIDES OR POLYSACCHARIDES
  • C13K1/00—Glucose; Glucose-containing syrups
  • C13K1/06—Glucose; Glucose-containing syrups obtained by saccharification of starch or raw materials containing starch
  • C13K1/08—Purifying

Definitions

• the present invention relates to the non-food and non-pharmaceutical use of an anhydrous dextrose composition, notably selected by its particle size and hygroscopicity characteristics.
• an “anhydrous dextrose composition” refers to any solid composition of glucose which has, a) a water content at most equal to 1%, preferably at most equal to 0.9%, expressed relatively to the weight of said composition and b) a D-glucose content at least equal to 96%, preferably at least equal to 97%, expressed relatively to the dry weight of said composition.
• This composition may have variable crystalline rates.
• this anhydrous form may be represented by very variable percentages of the alpha-anhydrous and beta-anhydrous forms, respectively.
• the anhydrous alpha form accounts for more than 85% by weight (dry weight/dry weight) of anhydrous dextrose.
• Non-food and non-pharmaceutical use refers to all uses in all fields of application, except the particular cases where the dextrose composition is intended to be directly ingested by humans or animals or intended to be directly injected to humans or animals.
• a selected dextrose composition has now been found capable of meeting the set of aforementioned criteria 1)-6) and consequently applicable in a multitude of uses such as those listed earlier.
• the particle size of the dextrose composition is conventionally measured by laser particle size analysis in a dry phase, for example on a particle size analyzer LASER LS 230 of the COULTER® brand fitted with a “dry powder” type dry phase module.
• the hygroscopic index corresponds to the difference in water content values of the dextrose composition, measured at equilibrium, on a same sample when the latter is placed at a temperature of 20° C. and at a relative humidity (RH) of 75% on the one hand and at 20° C. and at 50% RH on the other hand, it being understood that said sample is placed at 20° C., first at 50% RH, and then at 75% RH.
• RH relative humidity
• the apparent density corresponds to the unpacked density of dextrose composition expressed in kg/l, and is measured with any standard method.
• the dextrose composition which may be used according to the invention has a particle size such that at most 3%, preferably at most 2%, of its particles have a size at most equal to 40 microns.
• this value may be less than 1.5% and notably be between 0 and 1%.
• said composition has a particle size such that at most 7%, preferably at most 6%, of its particles have a size at most equal to 100 microns. This value may be less than 5%, even being located between 0 and 3%.
• said composition has a particle size such that:
• the average diameter (in this case D (4,3)) of the constitutive particles of said dextrose composition may notably be larger than 250 microns, and less than 650 microns, in particular be between 280 and 540 microns. As an example, it may be located between 300 and 500 microns, notably between 350 and 500 microns.
• said dextrose composition which may be used according to the invention, has:
• the hygroscopic index may significantly be less than 0.15%, notably less than 0.1% and for example between 0.01 and 0.09%.
• anhydrous dextrose composition which may be used according to the invention, was able, at a very high RH, i.e., 85%, to contain less than 1% water, or even less than 0.5% water, at equilibrium.
• the apparent density of said composition may advantageously be between 0.80 and 0.92 kg/l.
• an anhydrous dextrose composition as defined earlier, but having a D-glucose content even higher than 96 or 97%, and/or a water content even lower than 1 or 0.9%.
• the dextrose composition has:
• the D-glucose content may be between 99.5% and 100%. It may notably be larger than 99.7% (dry weight/dry weight).
• Glucose may in majority, or even quasi-exclusively, be present in a crystalline anhydrous form, whereby it itself may in majority or even quasi-exclusively, be an alpha anhydrous form.
• the water content may, for example, be between 0.05 and 0.4%. It may notably be less than 0.2%.
• anhydrous dextrose composition which may be used according to the invention, said composition generally appears as a powder which may be termed “free flowing powder”.
• test T said composition may have improved flow characteristics as opposed to those of dextrose compositions generally put on the market, notably in the fields of application mentioned herein.
• said composition may advantageously have, according to said T test, a flow index such as it will be defined elsewhere, less than 25 seconds, preferably between 8 and 24 seconds, and notably between 9 and 22 seconds. This index value may notably be between 10 and 18 seconds.
• the anhydrous dextrose composition which may be used according to the invention, has very low compressibility, or even a lack of compressibility.
• said composition may notably have a compressibility, as determined according to the A test as described in paragraph 28, page 3, lines 30-35 of EP 1 013 777, of less than 80 Newtons, preferably less than 50 Newtons, and even more preferentially less than 30 Newtons.
• This A test consists of measuring the force, expressed in Newton, which is representative of the compressibility of the investigated powder dextrose.
• this force expresses the crushing strength of a tablet which is cylindrical with convex faces (radius of curvature of 14 mm), of a diameter of 13 mm, of a thickness of 6 mm and of a weight of 0.764 g, i.e., and of an apparent density of 1.3 kg/l.
• the anhydrous dextrose composition simultaneously has:
• a dextrose composition characterized in this way is novel, independently of the applications (whether food, pharmaceutical applications) for which it may be intended.
• such a novel industrial product further has:
• the anhydrous dextrose composition according to the invention or which may be used according to the invention may be obtained by any means or any combination of means, capable of giving it the selected aforementioned characteristics a)-c) of particle size, hygroscopic index and apparent density, respectively, as well as possibly optional characteristics of D-glucose content, water content, average diameter and/or compressibility, also mentioned earlier.
• It may notably be prepared from a very high glucose syrup (96% as expressed in dry weight/dry weight) as initially obtained according to general principles described in any of the patents FR 2 762 616, FR 2 791 700, FR 2 791 701, FR 2 791 703 or FR 2 830 021 in the name of the applicant, in particular from a syrup as initially obtained by applying membrane means, in particular nanofiltration membranes or chromatographic means.
• Said syrup may then advantageously be concentrated and crystallized by evaporation as described for example in the aforementioned FR 2 791 703 patent.
• the resulting mass of crystals may for example then be dried on a rotary drum and/or a fluidized bed so that its water content is at most equal to 1%, for example of the order of 0.05 to 0.40%, notably in order to obtain a composition free or quasi-free of dextrose monohydrate and having a hygroscopic index as selected.
• the thereby dried crystals may then undergo at least one physical separation step, for example at least one separation step on one or more industrial sieves, whereby the mesh size for each of them will be carefully selected so that a powder having not only the particle size but even the density characteristics according to the invention may be recovered.
• at least one physical separation step for example at least one separation step on one or more industrial sieves, whereby the mesh size for each of them will be carefully selected so that a powder having not only the particle size but even the density characteristics according to the invention may be recovered.
• the selected anhydrous dextrose composition according to the invention finds an immediate industrial application in the preparation of compositions, notably nutritive, dehydrating, conditioning and preservative and/or protective compositions, intended for treating plants or portions of plants, for example cut flowers.
• the glucose or dextrose is conventionally associated i.a. with at least one organic acid such as citric acid or succinic acid and with at least one biocidal agent.
• An anhydrous dextrose composition according to the invention is prepared from a mass of dextrose crystals having a D-glucose content larger than 99.5% (dry weight/dry weight) and a water content of about 3%, said bulk of crystals having been obtained after conventional steps, conducted continuously, of crystallization by evaporation, water removal (separation of the crystals and of the mother liquors), washing of the crystals, than final water removal from the washed crystals.
• crystals are then dried on a rotary drum with hot air, so as to have a water content of less than 0.2%, and then cooled to room temperature on a fluidized bed.
• the anhydrous texture composition according to the invention represents the mass of dextrose crystals retained on this second sieve.
• This funnel has a conical portion, the height of which is 240 mm and its internal diameter is 200 mm, said conical portion being extended by a rectilinear portion, the height of which is 100 mm and its internal diameter is 20 mm.
• the end extremity of said rectilinear portion is fitted with a valve, in this case in the closed position, thereby obstructing this end extremity and thereby preventing flow of the powder.
• the stopwatch is stopped when the whole of the powder has finished flowing from the funnel. The time required for this flow is noted down.
• the flow index (“FLOW T”) according to the T test which has just been described, expressed in seconds, corresponds to the average of 3 measured values for the same tested composition.
• COMPOSITION A according to the invention thus has a FLOW T flow index of 14.32 seconds, it being specified moreover that said COMPOSITION A:
• test T′ Similar to test T except that the 1 kg mass of COMPOSITION A introduced into the standardized funnel is replaced by the same mass of a formulated composition consisting of a powder mixture based on:
• Such a mixture based on dextrose, an acidifying agent (GDL) and a biocidal agent (DCINa) may notably be used in the field of the compositions intended for treating plants or portions thereof, in particular cut flowers.
• COMPOSITION A with its physical characteristics may therefore advantageously be used for preparing formulated free flowing powder compositions.
• compositions A, B and C have remarkable characteristics in terms of particle size, hygroscopicity, density and flow, and may therefore be used advantageously, alone or as a mixture, as free flowing powders in as varied applications as those for synthesizing via a chemical or biotechnological route, substances, additives or active ingredients, for producing materials such as plaster boards, mineral binders or even for treating plants.

Landscapes

• Chemical & Material Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Health & Medical Sciences (AREA)
• Organic Chemistry (AREA)
• General Health & Medical Sciences (AREA)
• Emergency Medicine (AREA)
• Engineering & Computer Science (AREA)
• Biochemistry (AREA)
• Wood Science & Technology (AREA)
• Molecular Biology (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Environmental Sciences (AREA)
• Crystallography & Structural Chemistry (AREA)
• Agronomy & Crop Science (AREA)
• Pest Control & Pesticides (AREA)
• Plant Pathology (AREA)
• Dentistry (AREA)
• Zoology (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Materials Engineering (AREA)
• Medicinal Preparation (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)
• Saccharide Compounds (AREA)
• Medicines Containing Plant Substances (AREA)
• Jellies, Jams, And Syrups (AREA)
• Seasonings (AREA)

Applications Claiming Priority (2)

Publications (2)

Family

ID=34954252

Family Applications (1)

Country Status (8)

Citations (16)

Family Cites Families (3)

• 2004
  • 2004-10-29 FR FR0411603A patent/FR2877186B1/fr active Active
• 2005
  • 2005-10-25 DE DE602005025299T patent/DE602005025299D1/de active Active
  • 2005-10-25 AT AT05292253T patent/ATE491812T1/de not_active IP Right Cessation
  • 2005-10-25 EP EP05292253A patent/EP1652938B1/fr active Active
  • 2005-10-27 NO NO20055003A patent/NO20055003L/no not_active Application Discontinuation
  • 2005-10-28 JP JP2005315325A patent/JP5047489B2/ja active Active
  • 2005-10-28 US US11/260,268 patent/US7731991B2/en active Active
  • 2005-10-28 KR KR1020050102359A patent/KR20060059804A/ko not_active Application Discontinuation

Patent Citations (25)

Non-Patent Citations (4)

Also Published As

Similar Documents

Legal Events